Clinical Trials Directory

Trials / Completed

CompletedNCT00270335

Optimizing Propofol in Obese Patients

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
38 (actual)
Sponsor
Rigshospitalet, Denmark · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

An accurate dosage of anesthetics during surgery is important. Usually this is achieved through close observation of the patient, but a new monitor (CSM-monitor) can measure the level of anesthesia more closely. In obese patients dosage of drugs is difficult due to the change in body composition. The CSM-monitor may provide a more accurate dosage of propofol (an anesthetic agent) during surgery, and as a consequence of that, also reduce the postoperative need for analgesics. Main objective: To optimise propofol dosing in obese patients undergoing hysterectomy. Main hypothesis: Monitoring the depth of anesthesia using the CSM-monitor reduces time to opening eyes in obese patients after hysterectomy in propofol anesthesia. Secondary hypotheses: CSM-monitoring reduce propofol dose in obese patients undergoing hysterectomy. Patients with a high CSM-level during hysterectomy have higher postoperative consumption of analgesics. Supplementary, an algorithm for the dose of propofol that most frequently results in a CSM-level between 40 and 60 is calculated.

Conditions

Interventions

TypeNameDescription
DRUGPropofol

Timeline

Start date
2006-01-01
Primary completion
2007-08-01
Completion
2007-08-01
First posted
2005-12-26
Last updated
2009-10-16

Locations

2 sites across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00270335. Inclusion in this directory is not an endorsement.